Fringed micelle model, crystalline-amorphous

If the ordered, crystalline regions are cross sections of bundles of chains and the chains go from one bundle to the next (although not necessarily in the same plane), this is the older fringe-micelle model. If the emerging chains repeatedly fold buck and reenter the same bundle in this or a different plane, this is the folded-chain model. In either case the mechanical deformation behavior of such complex structures is varied and difficult to unravel unambiguously on a molecular or microscopic scale. In many respects the behavior of crystalline polymers is like that of two-ph ise systems as predicted by the fringed-micelle- model illustrated in Figure 7, in which there is a distinct crystalline phase embedded in an amorphous phase (134). 

The traditional model used to explain the properties of the (partly) crystalline polymers is the "fringed micelle model" of Hermann et al. (1930). While the coexistence of small crystallites and amorphous regions in this model is assumed to be such that polymer chains are perfectly ordered over distances corresponding to the dimensions of the crystallites, the same polymer chains include also disordered segments belonging to the amorphous regions, which lead to a composite single-phase structure (Fig. 2.10). 

The fringed micelle model gives an extremely simple interpretation of the "degree of crystallinity" in terms of fractions of well-defined crystalline and amorphous regions. Many excellent correlations have evolved from this model through the years, so that it has long been popular. 

In the present concept of the structure of crystalline polymers there is only room for the fringed micelle model when polymers of low crystallinity are concerned. For polymers of intermediate degrees of crystallinity, a structure involving "paracrystals" and discrete amorphous regions seems probable. For highly crystalline polymers there is no experimental evidence whatsoever of the existence of discrete amorphous regions. Here the fringed micelle model has to be rejected, whereas the paracrystallinity model is acceptable. 

By contrast, total molecular architecture, involving the conjunction of crystalline and amorphous parts, has proved to be much less amenable to investigation. For a long time structural interpretations were based on the fringed-micelle model in which molecules are supposed to wander through... 

Flgure 2.1 Conformational differences of polymer chains in the amorphous and crystalline states. Fringed micelle model. Parallel and coiled lines represent, respectively, portions of chains in the crystalline and the amorphous regions. 

Some cotton cellulose is noncrystalline or amorphous in the sense of lacking definite crystalline form. One reason is that cotton cellulose has a broad molecular weight distribution, making high-crystalline perfection impossible. The small crystallites constitute deviations from ideal crystals that are infinite arrays. The remaining amorphous character of most polymers is often thought to arise from the fringed micelle model of the solid structure. In... 

For convenience, we can regard an isotropic semicrystalline polymer as being made up of an isotropic polycrystalline phase and an isotropic amorphous phase, as shown in Fig. 6, which is purely diagrammatic (it shows the classical fringed micelle model for simplicity). From a geometrical standpoint, we cannot discriminate a priori between two continuous interpenetrating phases, a dispersion of a crystalline phase in an amorphous phase, or of an amorphous phase in a crystalline phase. The distinction may depend upon the volume fractions. 

Figure 1.6. Fringed micelle model. Note alternating crystalline and amorphous regions. (Bryant, 1947.)...

Fig. 1-28 Schematic diagram of the fringed micelle model of polymer amorphous-crystalline structure [44,45].

Fig. 2.5. Chain molecules in (A) amorphous, (B) crystalline and (C) semicrystalline regions of polymers (fringed micelle model).

The first model to describe the structure of a semi-crystalline polymer was the so-called fringed micelle model (Figure 1.11), which is a natural development of the imagined situation in an amorphous polymer. The molecular chains alternate between regions of order (the crystallites) and disorder (the amorphous regions). 

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